HRID417174

反应详情

EQUATION

反应方程式

HRID 417174 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of [3,3-dimethyl-but-(E)-ylideneamino]-acetic acid tert-butyl ester (3.37 g, 15.8 mmol) prepared in Example 1 and E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-1,3-dihydro-indol-2-one (4 g, 13 mmol) prepared in Example 2 in dichloromethane (100 mL) were added triethylamine (6.6 mL, 47.4 mmol) and AgF (2 g, 15.8 mmol). The mixture was stirred at room temperature for 18 h. The mixture was concentrated, and the residue was partitioned between ethyl acetate and brine. The organic layer was separated, washed with water, dried over MgSO4, and concentrated. The residue was dissolved into t-butanol (30 mL), and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, Fluka) (7.2 g, 47.4 mmol) was added. The reaction mixture was heated at 120° C. for 2 h. The mixture was then cooled to room temperature and concentrated. The residue was partitioned between ethyl acetate and water. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with water, brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:3, 1:2) to give as rac-(2′S,3′R,4′S,5′R)-6-chloro-4′-(3-chloro-2-fluoro-phenyl)-2′-(2,2-dimethyl-propyl)-2-oxo-1,2-dihydro-spiro[indole-3,3′-pyrrolidine]-5′-carboxylic acid tert-butyl ester a white foam (2.7 g, 33%)

WORKUP

后处理

  1. concentrationThe mixture was concentrated
  2. customthe residue was partitioned between ethyl acetate and brine
  3. customThe organic layer was separated
  4. washwashed with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. additionwas added
  8. temperatureThe reaction mixture was heated at 120° C. for 2 h
  9. temperatureThe mixture was then cooled to room temperature
  10. concentrationconcentrated
  11. customThe residue was partitioned between ethyl acetate and water
  12. customThe organic layer was separated
  13. extractionthe aqueous layer was extracted with ethyl acetate
  14. washwashed with water, brine
  15. dry with materialdried over MgSO4
  16. concentrationconcentrated
  17. customThe residue was purified by chromatography (EtOAc:hexanes=1:3, 1:2)